Osteosarcoma: Cells-of-Origin, Cancer Stem Cells, and Targeted Therapies

被引:179
作者
Abarrategi, Ander [1 ]
Tornin, Juan [2 ,3 ]
Martinez-Cruzado, Lucia [2 ,3 ]
Hamilton, Ashley [1 ]
Martinez-Campos, Enrique [4 ]
Rodrigo, Juan P. [2 ,3 ]
Victoria Gonzalez, M. [2 ,3 ]
Baldini, Nicola [5 ,6 ]
Garcia-Castro, Javier [7 ]
Rodriguez, Rene [2 ,3 ]
机构
[1] Francis Crick Inst, Haematopoiet Stem Cell Lab, London WC2A 3LY, England
[2] Cent Univ Hosp Asturias HUCA, Oviedo 33011, Spain
[3] Inst Oncol Asturias IUOPA, Oviedo 33011, Spain
[4] Univ Complutense Madrid, E-28040 Madrid, Spain
[5] Rizzoli Orthopaed Inst, Orthopaed Pathophysiol & Regenerat Med Unit, I-40136 Bologna, Italy
[6] Univ Bologna, Dept Biomed & Neuromotor Sci, I-40123 Bologna, Italy
[7] Inst Hlth Carlos III ISCIII, Cellular Biotechnol Lab, Madrid 28220, Spain
关键词
TUMOR-INITIATING CELLS; SIDE POPULATION CELLS; C-FOS; INHIBITS OSTEOSARCOMA; DRUG-RESISTANCE; GENE-EXPRESSION; LUNG METASTASIS; MESSENGER-RNA; STROMAL CELLS; SELF-RENEWAL;
D O I
10.1155/2016/3631764
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Osteosarcoma (OS) is the most common type of primary solid tumor that develops in bone. Although standard chemotherapy has significantly improved long-term survival over the past few decades, the outcome for those patients with metastatic or recurrent OS remains dismally poor and, therefore, novel agents and treatment regimens are urgently required. A hypothesis to explain the resistance of OS to chemotherapy is the existence of drug resistant CSCs with progenitor properties that are responsible of tumor relapses and metastasis. These subpopulations of CSCs commonly emerge during tumor evolution from the cell-of-origin, which are the normal cells that acquire the first cancer-promoting mutations to initiate tumor formation. In OS, several cell types along the osteogenic lineage have been proposed as cell-of-origin. Both the cell-of-origin and their derived CSC subpopulations are highly influenced by environmental and epigenetic factors and, therefore, targeting the OS-CSC environment and niche is the rationale for many recently postulated therapies. Likewise, some strategies for targeting CSC-associated signaling pathways have already been tested in both preclinical and clinical settings. This review recapitulates current OS cell-of-origin models, the properties of the OS-CSC and its niche, and potential new therapies able to target OS-CSCs.
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页数:13
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